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Neurogenetics

Showing results (501-510 of 1,081) with videos related to

Pageof 109
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Neurogenetics|June 7, 2024
Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory CenterElka Stefanova, Ana Marjanović, Valerija Dobričić, et al.
Neurogenetics|February 10, 2026
A novel heterozygous mutation of BCL11B gene causes neurodevelopmental disorder and middle type hypospadias in a Chinese boy with 5 years follow-upYawen Liu, Zhen Pan, Jiarui Shi, et al.
Neurogenetics|January 30, 2026
A de novo KCNA3 and an inherited KCNQ3 missense variant causing a developmental and epileptic encephalopathy, intellectual disability, and behavioral anomaliesEnrica Marchionni, Vito Luigi Colona, Emanuele Agolini, et al.
Neurogenetics|December 9, 2025
LAMB1-associated leukoencephalopathy: a continuum from a prenatal, recessive syndrome to a dominant, adult-onset disorderJosé Zamora, Víctor Faundes
Neurogenetics|December 2, 2025
L-DOPA in diurnal fluctuating dystonia: two different clinical presentations, one treatmentBeyza Karataş, Ayten Güleç, Ömer YiğitSezer, et al.
Neurogenetics|December 26, 2024
Brain malformation, neurodevelopmental disorder and epilepsy in a case of two rare genetic diseases: overlapping phenotypeEmine Karatas, Ayten Gulec, Maide Korkmaz, et al.
Neurogenetics|January 15, 2025
Neuronal ceroid lipofuscinosis 11 (CLN11) presenting with early-onset cone-rod dystrophy and learning difficultiesGustavo Maximiano-Alves, Renata do Amaral Moreto Caravelas, Trajano Aguiar Pires Gonçalves, et al.
Neurogenetics|January 17, 2025
Neuroinflammation and neurodegeneration in Huntington's disease: genetic hallmarks, role of metals and organophosphatesOmkar Kumar Kunwar, Shamsher Singh
Neurogenetics|January 6, 2025
Computational modeling design of novel NMDAR agonist for the treatment of SchizophreniaAmena Khatun Manica, Mariam Omowunmi Daud, Michael Olanrewaju Faloyo, et al.
Neurogenetics|March 19, 2024
Whole exome sequencing in Serbian patients with hereditary spastic paraplegiaMarija Brankovic, Vukan Ivanovic, Ivana Basta, et al.
Pageof 109

Showing results (501-510 of 1,081) with videos related to

Sort By:
Pageof 109
Neurogenetics|June 7, 2024
Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory CenterElka Stefanova, Ana Marjanović, Valerija Dobričić, et al.
Neurogenetics|February 10, 2026
A novel heterozygous mutation of BCL11B gene causes neurodevelopmental disorder and middle type hypospadias in a Chinese boy with 5 years follow-upYawen Liu, Zhen Pan, Jiarui Shi, et al.
Neurogenetics|January 30, 2026
A de novo KCNA3 and an inherited KCNQ3 missense variant causing a developmental and epileptic encephalopathy, intellectual disability, and behavioral anomaliesEnrica Marchionni, Vito Luigi Colona, Emanuele Agolini, et al.
Neurogenetics|December 9, 2025
LAMB1-associated leukoencephalopathy: a continuum from a prenatal, recessive syndrome to a dominant, adult-onset disorderJosé Zamora, Víctor Faundes
Neurogenetics|December 2, 2025
L-DOPA in diurnal fluctuating dystonia: two different clinical presentations, one treatmentBeyza Karataş, Ayten Güleç, Ömer YiğitSezer, et al.
Neurogenetics|December 26, 2024
Brain malformation, neurodevelopmental disorder and epilepsy in a case of two rare genetic diseases: overlapping phenotypeEmine Karatas, Ayten Gulec, Maide Korkmaz, et al.
Neurogenetics|January 15, 2025
Neuronal ceroid lipofuscinosis 11 (CLN11) presenting with early-onset cone-rod dystrophy and learning difficultiesGustavo Maximiano-Alves, Renata do Amaral Moreto Caravelas, Trajano Aguiar Pires Gonçalves, et al.
Neurogenetics|January 17, 2025
Neuroinflammation and neurodegeneration in Huntington's disease: genetic hallmarks, role of metals and organophosphatesOmkar Kumar Kunwar, Shamsher Singh
Neurogenetics|January 6, 2025
Computational modeling design of novel NMDAR agonist for the treatment of SchizophreniaAmena Khatun Manica, Mariam Omowunmi Daud, Michael Olanrewaju Faloyo, et al.
Neurogenetics|March 19, 2024
Whole exome sequencing in Serbian patients with hereditary spastic paraplegiaMarija Brankovic, Vukan Ivanovic, Ivana Basta, et al.
Pageof 109